Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Heat developable image recording material

a technology of developing photosensitive materials and recording materials, which is applied in the direction of photosensitive materials, electrographic processes, instruments, etc., can solve the problems of deterioration of the preservation property of row photosensitive materials, no satisfactory output system for obtaining medical images, and sensitivity decrease during preservation, etc., to achieve excellent image preservation properties

Inactive Publication Date: 2003-10-09
FUJIFILM HLDG CORP
View PDF10 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0145] An alkyl group, an aryl group, an alkoxy group and an aryloxy group are preferable as R.sup.21, R.sup.22 and R.sup.23. It is preferable in terms of the effect of the invention that at least one of R.sup.21, R.sup.22 and R.sup.23 is an alkyl group or an aryl group, and it is more preferable that at least two of them are alkyl or aryl groups. Preferably, groups represented by R.sup.21, R.sup.22 and R.sup.23 are the same groups for purchasing the reagents with cheap price.
[0146] While examples (exemplified compounds 3-1 to 3-17) of the compounds capable of forming hydrogen bonds such as the compounds represented by the general formula (3) in the invention, the invention is not restricted thereto. 202122
[0147] Examples of the hydrogen bond forming compounds other than those described above are described in EP NO. 1096310, and Japanese Patent Application Nos. 2000-270498 and 2000-124796.
[0148] The compound represented by the general formula (3) to be used in the invention may be used in the photosensitive material by adding in an application fluid in any form such as in solution, in emulsified dispersion and solid micro-dispersion as in the case of the reducing agent. The compounds form hydrogen bonding complexes with compounds having phenolic hydroxyl groups or amino groups, and the complex may be isolated in a crystalline state depending on the combination between the reducing agents and the compounds represented by the general formula (3). For obtaining stable performance, it is particularly preferable to use the crystalline powder isolated as described above as a dispersion of solid fine particles. In a different metod preferably used, the reducing agent and the compound represented by the general formula (3) are mixed as powders, and the complex is formed when they are dispersed with a sand grinder mill using an appropriate dispersing agent.
[0149] The compound represented by the general formula (3) is preferably used in a range of 1 to 200 mol %, more preferably in the range of 10 to 150 mol %, and still more preferably in the range of 30 to 100 mol %, relative to the reducing agent.
[0150] The halogen composition of the photosensitive silver halide to be used in the invention is not particularly restricted, and silver chloride, silver chlorobromide, silver bromide, silver iodobromide and silver iodochlorobromide may be used. Silver bromide and silver iodobromide are preferable among them. Distribution of the halogen composition in the particles may be uniform, may be discretely changed, or may be continuously changed. Silver halide particles having a core-shell structure may be preferably used. Preferably used core-shell structures include double to five-fold structures, more preferably double to four-fold structures. Preferably, a technology can be applied in which silver bromide or silver iodide is localized on the surface of the silver chloride, silver bromide or silver chlorobromide particles.

Problems solved by technology

Although various hard copy systems taking advantage of pigments and dyes, such as ink-jet printers and electrophotographic systems, are commercially available today, none of them are satisfactory as output systems for obtaining medical images.
Accordingly, although it is necessary to reduce the size of the silver halide particle and increase the number of particles while compensating its sensitivity by applying chemical sensitization, it was a problem that preservative property of row photosensitive materials are deteriorated and sensitivity decreases during preservation.
However, when the preservation conditions are very severe for the heat developable photosensitive material, for example when processed films are placed in a vehicle for transportation or the like in summer, troubles such as color changes throughout the film or transfer of characters printed on a bag as a container of the film onto the film may occur.
However, the commercially available heat developable photosensitive materials involve the problem in the image preserving property that causes fogging by light and heat after development.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Heat developable image recording material
  • Heat developable image recording material
  • Heat developable image recording material

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0340] (Preparation of PET Substrate)

[0341] PET with a specific viscosity IV of 0.66 (as measured in a mixed solvent of phenol and tetrachlotoethane in a ratio of 6:4 (mass ratio) at 25.degree. C.) was obtained by a conventional method using terephthalic acid and ethylene glycol. The polymer was formed into a pellet, dried at 130.degree. C. for 4 hours, and was extruded from a T type die after melting at 300.degree. C. followed by quenching, thereby obtaining a non-drawn film with a thickness of 175 .mu.m after heat curing.

[0342] The film was drawn 3.3 times using three rolls with different circumference speeds with each other in the longitudinal direction, and subsequently drawn 4.5 times in the transverse direction using a tenterhook. The temperatures for both draw treatments were 110.degree. C. and 130.degree. C., respectively. After heat-curing the film at 240.degree. C. for 20 seconds, it was relaxed by 4% in the transverse direction at the same temperature. After slitting the ...

example 2

[0467] >

[0468] The heat developable image recording material-19 was prepared by the same method as in the heat developable image recording material-9, except that the emulsion layer (photosensitive layer) application fluid-9 was changed to the emulsion layer application fluid-19, and the yellow pigment compound 15 was eliminated from the halation preventive layer.

[0469] The amount of application (g / m.sup.2) of each compound in the emulsion layer was as follows.

5 organic acid silver salt dispersion F 6.19 pigment (C. I. Pigment Blue 60) 0.036 organic polyhalogen compound-2 0.13 organic polyhalogen compound-3 0.41 phthalazine compound-1 0.21 SBR latex 11.1 reducing agent complex-3 1.54 mercapto compound (1-17) 0.002 silver halide (as Ag) 0.10

[0470] The heat developable image recording materials-11 to 18 and 20 were prepared by the same method as in the heat developable image recording material-19, except that the organic acid silver salt dispersion F of the heat developable image reco...

example 3

[0473] >

[0474] The emulsion layer (photosensitive layer) application fluid-9 in the heat developable image recording material-9 was changed to the emulsion layer (photosensitive layer) application fluid-29, and the yellow pigment compound 15 was eliminated from the halation preventive layer. The fluorine based surfactants F-1, F-2, F-3 and F-4 in the protective second layer and back face protective layer were changed to F-5, F-6, F-7 and F-8, respectively, with the same weight. The heat developable image recording material-29 was prepared by the same method as in the heat developable image recording material-9 except the conditions above.

[0475] The amount of application (g / m.sup.2) of each compound in the emulsion layer was shown in Table 4.

7 organic silver halide dispersion F 5.57 pigment (C. I. Pigment Blue 60) 0.032 reducing agent-4 0.40 reducing agent-5 0.36 organic polyhalogen compound-2 0.12 organic polyhalogen compound-3 0.37 phthalazine compound-1 0.19 SBR latex 10.0 hydroge...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
carbon numberaaaaaaaaaa
temperatureaaaaaaaaaa
temperatureaaaaaaaaaa
Login to View More

Abstract

A heat developable image recording material including a photosensitive silver halide, a reducing agent for silver ions, a binder and non-photosensitive organic acid silver salt particles on one side of the surface of a substrate. A content of silver behenate in the non-photosensitive organic acid silver salt particles is 90 mol % to 100 mol %, and at least one kind of mercapto compound is contained in a surface of the substrate at the same side as a layer having the photosensitive silver halide. The heat developable image recording material includes a compound represented by following the general formula (1) wherein, R<21>, R<22 >and R<23 >each independently represent a substituted or non-substituted alkyl group. When R21, R<22 >or R<23 >have a substituent, the substituent is a halogen atom etc. The non-photosensitive organic particles are prepared from organic acids including at least behenic acid and erucic acid, and a content of the erucic acid is 0.000001 mol % to 0.4 mol %.

Description

[0001] 1. Field of the Invention[0002] The present invention relates to a heat developable photosensitive image recording material (simply referred to as a heat developable photosensitive material hereinafter).[0003] 2. Description of the Related Art[0004] Reduction of the amount of waste after development and fixing of films for medical diagnostics and photographic printing has been strongly demanded in recent years in view of environmental preservation and for saving work spaces. Accordingly, technologies related to heat developable photosensitive materials are urgently required for providing films for medical diagnosis and photographic printing, by which efficient exposure is possible using a laser image setter or laser imager to form clear images with high resolution and sharpness. No liquid chemicals are needed for development and fixing when the heat developable photosensitive material is used, making it possible to supply to customers a heat development system that is more si...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): G03C1/498
CPCG03C1/49809G03C1/49827G03C1/49845G03C2200/43G03C2001/0157G03C2200/40
Inventor FUJIWARA, ITSUOYAMAMOTO, SEIICHIOYAMADA, TAKAYOSHI
Owner FUJIFILM HLDG CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products